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Behavioural Intervention

BESST + Standard Care for Suicide Prevention

N/A
Recruiting
Led By Natalie Riblet, MD, MPH
Research Sponsored by White River Junction Veterans Affairs Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be 18 years or older
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to 3 months post-discharge
Awards & highlights

Study Summary

This trial will assess if a suicide prevention program (BESST) combined with standard care reduces suicide-related outcomes in rural Veterans discharged from mental health care.

Who is the study for?
This trial is for Veterans over 18, recently discharged from VA community mental health care, at risk of self-harm, and connected to specific VAMCs. They must speak English and be able to consent. Those not clinically appropriate or in vulnerable groups won't be included.Check my eligibility
What is being tested?
The study tests the BESST suicide prevention program alongside standard care against standard care alone for rural Veterans post-discharge. It involves an educational session, follow-up check-ins, and assessments over three months to see if BESST improves outcomes.See study design
What are the potential side effects?
Since this trial focuses on a psychological intervention (BESST), traditional physical side effects are not applicable. However, participants may experience emotional discomfort discussing sensitive topics during sessions.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am 18 years old or older.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to 3 months post-discharge
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline to 3 months post-discharge for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Suicidal Ideation: The Beck Scale for Suicidal Ideation (BSS)
Secondary outcome measures
Connectedness: Interpersonal Needs Questionnaire-15 (INQ-15)
Hopelessness: Beck Hopelessness Scale (BHS)
Patient Engagement: General Self-Efficacy Scale (GSES)
+3 more

Trial Design

2Treatment groups
Experimental Treatment
Group I: ControlExperimental Treatment1 Intervention
Patients randomized to the control arm will receive standard mental health care alone.
Group II: BESSTExperimental Treatment2 Interventions
Patients randomized to the BESST intervention arm will receive the BESST intervention combined with standard mental health care.

Find a Location

Who is running the clinical trial?

White River Junction Veterans Affairs Medical CenterLead Sponsor
28 Previous Clinical Trials
16,856 Total Patients Enrolled
2 Trials studying Suicide Prevention
152 Patients Enrolled for Suicide Prevention
VHA Office of Rural HealthUNKNOWN
Natalie Riblet, MD, MPHPrincipal InvestigatorWhite River Junction VA Medical Center

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is this trial still open to enrollment?

"Yes, according to clinicaltrials.gov the trial is actively accepting participants with a start date of October 1st 2023 and most recent update being November 14th 2023. 25 individuals are required for this study at one medical center."

Answered by AI

How many individuals are currently enrolled in this clinical trial?

"Affirmative. Clinicaltrials.gov corroborates that this research is presently welcoming participants, having been posted on October 1st 2023 and updated recently as of November 14th 2023. 25 patients are required for the trial at one medical centre."

Answered by AI
~11 spots leftby Sep 2024